Center For Medical Genetics Ghent - Nextflow workflows's repositories
structural
A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region expansions (RREs) from short DNA reads
nextflow-beginner-feb-2024
The repository used at the Beginner Nextflow course in february 2024
preprocessing
Preprocessing workflow for sequencing data at CMGG
configs
Nextflow config files
MIT000
qdnaseq
A Nextflow pipeline to create qDNAseq bin annotations
Language:NextflowMIT000
sampletracking
CMGG Sampletracking workflow
Language:NextflowMIT000
test-datasets
Test datasets for unit tests with the nf-cmgg pipelines
wisecondorx
A nextflow pipeline for creating references for WisecondorX